TECHNICAL FIELD
[0001] The present invention relates to a medicament delivery device and more particularly
to the medicament delivery device with automatic functions.
BACKGROUND
[0002] Medicament delivery devices such as auto-injectors, inhalers, on-body devices are
generally known for the self-administration of a medicament by patients without formal
medical training occurs. For example, those patients suffering from diabetes or those
people are taking the artificial fertilization procedure may require repeated injections
of insulin or hormone. Other patients may require regular injections of other types
of medicaments, such as a growth hormone.
[0003] Medicament delivery devices may be delivery to end users with prefilled medicament
containers. A medicament container usually constructed by a glass or plastic barrel
with a stopper sealing on its rear end and a delivery member arranged on its front
end; or a pierceable membrane arranged on its front end. Most of time, the medicament
container will be filed with specific medicament first, then be assembled into a medicament
delivery device. The medicament delivery device usually comprises a plunger rod configured
to push on the stopper of the medicament container to deliver the contained medicament
to an end user. However, when the medicament is filing into medicament containers
and stoppers are placing to seal medicament containers, the position of stoppers in
each medicament container might be different. The difference is caused by multiple
factors, such as the manufacture temperature and/ or pressure, the spread of silicone
oil in medicament containers, the surface tension force of the medicament and/ or
the delivery member. Even a batch of medicament containers have been perfectly filed
with the medicament and position of each stopper are all the same, when the batch
is shipping to a market distributer or a medicament delivery device manufacturer through
air transport, those positions of each stopper may change due to the pressure difference.
Since the difference of the stopper position in each medicament container, a plunger
rod in a medicament delivery device usually be arranged rearward and has a gap to
the stopper of the assembled medicament container. Otherwise, if the plunger rod is
arranged too close to the stopper of the assembled medicament container, there may
be a risk that the plunger rod squeezes the stopper during assembling or during shipping
by air transport which may result as the damage of the medicament container due to
the increased interior pressure or contamination by a leakage of the contained medicament.
[0004] However, the length size of the gap dependent on the position of the stopper and
may be different in each assembled medicament delivery device, therefore, a risk of
dose inaccuracy may be raised. A medicament delivery device required high delivered
dose accuracy usually will arranged with an overfilled medicament container and a
plunger rod with specific hard stop arrangement. The delivered dose is determined
by the travel distance of the plunger rod, not the entire amount of the medicament
contained in the medicament. However, with the difference of the length size of the
gap between the front end of the plunger rod and the rear end of the stopper of the
medicament container, the delivered dose is actually determined by subtracting the
length size of the gap from the travel distance of the plunger rod; therefore, the
difference of the length size of the gap raises the risk of delivered dose inaccuracy.
[0005] The document
WO 2006/057604 discloses a medicament delivery device provided with a number of automatic functions,
which medicament delivery device has been very well received on the market. The medicament
delivery device comprises a rotator and a needle shield with a needle shield link,
the axial movement of the needle shield link is configured to run along ledges on
the outer surface of the rotator and causes the rotator to rotate. The rotation of
the rotator is arranged to release the biased plunger comprising a stop member that
resting on the inner ledge of the rotator.
[0006] In most instances this solution works very well. However, there is also a demand
to have a further improvement on the disclosed medicament delivery device.
SUMMARY
[0007] The aim of the present invention is to obtain alternative and more robust solutions.
[0008] In the present disclosure, when the term "distal direction" is used, this refers
to the direction pointing away from the dose delivery site during use of the medicament
delivery device. When the term "distal part/end" is used, this refers to the part/end
of the delivery device, or the parts/ends of the members thereof, which under use
of the medicament delivery device is/are located furthest away from the dose delivery
site. Correspondingly, when the term "proximal direction" is used, this refers to
the direction pointing towards the dose delivery site during use of the medicament
delivery device. When the term "proximal part/end" is used, this refers to the part/end
of the delivery device, or the parts/ends of the members thereof, which under use
of the medicament delivery device is/are located closest to the dose delivery site.
[0009] Further, the term "longitudinal", "longitudinally", "axially" or "axial" refer to
a direction extending from the proximal end to the distal end, typically along the
device or components thereof in the direction of the longest extension of the device
and/or component.
[0010] Similarly, the terms "transverse", "transversal", "transversally" refer to a direction
generally perpendicular to the longitudinal direction.
[0011] An object of this invention is provide a simple and reliable medicament delivery
device to perform an automatic calibration function.
[0012] According to an aspect of the invention, the object is achieved by a reliable medicament
delivery device according to claim 1.
[0013] There is hence provided a medicament delivery device, comprising: a housing having
a proximal end and a distal end; a medicament container arranged within the housing
and comprising a stopper and a delivery member; a biased delivery member cover associated
with the housing and movable in relation to the housing; a biased plunger rod associated
with the medicament container and movable in relation to the housing; a tubular rotator
associated with both the delivery member cover and the biased plunger rod; and a cap
assembly associated with the housing; wherein a gap is defined between the proximal
end of the biased plunger rod and the stopper of the medicament container when the
medicament delivery device is in an assembled state; and wherein the proximal end
of the biased plunger rod is in contact with the stopper of the medicament container
when the medicament delivery device is in a calibrated state..
[0014] According to one embodiment, the tubular rotator comprises a tubular body having
at least one retaining member on its inner surface.
[0015] According to one embodiment, the tubular rotator comprises a tubular body having
a first and a second retaining member on its inner surface
According to one embodiment, the biased plunger rod comprises a counter retaining
element configured to interact with the at least one retaining member or selectively
with each of the first, the second and the third retaining members.
[0016] According to one embodiment, the tubular rotator comprises a tubular body having
a retaining member on its inner surface; and the biased plunger rod comprises a first
and a second counter retaining elements, wherein the first and the second counter
retaining elements is configured to interact selectively with the retaining member.
[0017] According to one embodiment, the tubular rotator comprises a tubular body having
a first, a second and a third retaining member on its inner surface; and the biased
plunger rod comprises a counter retaining element, wherein the counter retaining element
is configured to interact selectively with each of the first, the second and the third
retaining members.
[0018] According to one embodiment, the retaining member is a radially inward protruding
rib.
[0019] According to one embodiment, the first and the second retaining members are ledges.
[0020] According to one embodiment, the counter retaining member is a radially outward protruding
arm.
[0021] According to one embodiment, the first and the second counter retaining members are
grooves.
[0022] According to one embodiment, the medicament delivery device further comprises a medicament
container configured to receive the medicament container.
[0023] According to one embodiment, the medicament container is axially fixed to the container
carrier.
[0024] According to one embodiment, the container carrier comprises a dose stop arranged
on its distal end.
[0025] According to one embodiment, the biased plunger rod further comprises an interaction
member configured to interact with a counter interaction member on the distal end
of the container carrier.
[0026] According to one embodiment, the interaction between the interaction member and the
counter interaction member is configured to provide a feedback to a user of the medicament
delivery device.
[0027] According to one embodiment, the biased delivery member cover comprises a guide element;
and the tubular rotator comprises a tubular body arranged with a guide track on its
outer surface; wherein the guide element is configured to interact with the guide
track such that an axial movement of the biased delivery member cover causes the tubular
rotator to rotate.
[0028] According to one embodiment, the biased delivery member cover comprises a delivery
member cover link; wherein the guide element is arranged on the delivery member cover
link.
[0029] According to one embodiment, the medicament delivery device is in the assembled state
when the rotator is in a first rotation position which is defined when the biased
plunger rod is in an initial position in which the counter retaining element is engaged
with the first retaining member; when the biased delivery member cover is in a first
retracted position in which the guide element is positioned on a first distal end
point of the guide track; and when the biased delivery member cover is held in said
position by the cap assembly which is releasably connected to the housing.
[0030] According to one embodiment, the medicament delivery device is in the assembled state
when the rotator is in a first rotation position which is defined when the biased
plunger rod is in an initial position in which the counter retaining element is engaged
with the first retaining member; when the biased delivery member cover is in a first
retracted position in which the guide element is positioned on a first distal end
point of the guide track; and when the biased delivery member cover is held in said
position by a knob assembly which axially fixed connected to the distal end of the
housing.
[0031] According to one embodiment, the medicament delivery device is in the calibrated
state when the rotator is in a second rotation position which is defined when the
biased plunger rod is in a calibrated position in which the counter retaining element
is engaged with the second retaining member, and when the biased delivery member cover
is in a first extended position in which the guide element is positioned on a first
proximal end point of the guide track after the cap assembly is removed from the housing.
[0032] According to one embodiment, the medicament delivery device is in the calibrated
state when the rotator is in a second rotation position which is defined when the
biased plunger rod is in a calibrated position in which the counter retaining element
is engaged with the second retaining member, and when the biased delivery member cover
is in a first extended position in which the guide element is positioned on a first
proximal end point of the guide track after the knob assembly is turned from a first
knob position to the second knob position.
[0033] According to one embodiment, the biased plunger rod is configured to move from the
calibrated position to a final position in which the counter retaining element is
engaged with the third retaining member, when the biased delivery member cover is
moved from the first extended position to a second retracted position in which the
guide element is positioned on a second distal end point of the guide track such that
the medicament contained in the medicament container is thereby delivered to a user
of the medicament delivery device.
[0034] According to one embodiment, the biased delivery member cover is axially movable
from the first retracted position to the first extended position; from the first extended
position to the second retracted position; and from the second retracted position
to a second extended position in which the guide element is positioned on a second
proximal end point of the guide track; such that the delivery member is extended from
the delivery member cover when the delivery member cover is in the first and the second
retracted positions; and is covered by the delivery member cover when the delivery
member cover is in the first and the second extended positions.
[0035] According to one embodiment, the counter retaining element is configured to disengage
with the second retaining member when the biased delivery member cover is axially
movable from the first extended position to the second retracted position such that
the rotator is moved from the second rotation position to a third rotation position.
[0036] According to one embodiment, the tubular rotator comprises a ramp surface arranged
between the first and the second retaining member; wherein the counter retaining element
is configured to move along the ramp surface from the first retaining member to the
second retaining member.
[0037] According to one embodiment, the axial movement of the biased delivery member cover
from the first retracted position to the first extended position causes the tubular
rotator to rotate from the first rotation position to the second rotation position.
[0038] According to one embodiment, the medicament delivery device comprises a resilient
member configured to proximally bias the biased delivery cover member.
[0039] According to one embodiment, the medicament delivery device can be an injection device,
an on-body device, an inhalation device, a nasal sprayer or a medical sprayer.
[0040] According to one embodiment, the delivery member can be an injection needle, a catheter
or a spray nozzle.
[0041] Other aspects, features, and advantages will be apparent from the summary above,
as well as from the description that follows, including the figures and the claims.
[0042] Generally, all terms used in the claims are to be interpreted according to their
ordinary meaning in the technical field, unless explicitly defined otherwise herein.
All references to "a/an/the element, apparatus, component, means, etc. are to be interpreted
openly as referring to at least one instance of the element, apparatus, component,
means, etc.", unless explicitly stated otherwise.
BRIEF DESCRIPTION OF THE DRAWINGS
[0043] The specific embodiments of the inventive concept will now be described, by way of
example, with reference to the accompanying drawings, in which:
Fig. 1 displays a medicament delivery device of the first embodiment of the invention.
Fig. 2 displays an exploded view the medicament delivery device of Fig. 1 in detail.
Fig. 3 displays a perspective view of a tubular rotator in the first embodiment.
Fig. 4 displays a perspective view of a plunger rod in the first embodiment.
Fig. 5 displays a dose stop in the first embodiment.
Fig. 6A-6B display a perspective and a side view of an outer arrangement of the tubular
rotator and a guide element on a delivery member cover in the first embodiment.
Fig. 7A-7B display cross section views of the medicament delivery device in an assembled
state and in a calibrated state in the first embodiment.
Fig. 8A-8B display perspective views of the arrangement of the cap assembly and the
delivery member cover in the second embodiment of the invention.
Fig. 9-10 display perspective views of a knob assembly in the third embodiment of
the invention.
Fig. 11 displays a perspective view of the outer arrangement of the tubular rotator
in the third embodiment.
Fig. 12 displays a cross-section view of the interaction between the guide element
and the knob assembly in the third embodiment.
Fig. 13 displays a perspective view of the outer arrangement of the tubular rotator
in the fourth embodiment of the invention.
Fig. 14 displays a perspective view of the interaction between the guide element,
the tubular rotator and the knob assembly in the fourth embodiment.
Fig. 15A-15B display cross-section views of the medicament delivery device in an assembled
state and in a calibrated state in the third and the fourth embodiment.
Fig. 16-17 display perspective views of a tubular rotator in an alternative embodiment
of the invention that the medicament delivery is arranged with auto penetration function.
Fig. 18-19 display perspective views of a retaining arrangement between the tubular
rotator and the plunger rod in an alternative embodiment of the invention.
DETAILED DESCRIPTION
[0044] The present application is directed to a feedback mechanism for a medicament delivery
device and will now be described more fully hereinafter with reference to the accompanying
drawings, in which exemplifying embodiments are shown. The feedback mechanism may,
however, be embodied in many different forms and should not be construed as limited
to the embodiments set forth herein; rather, these embodiments are provided by way
of example so that this disclosure will be thorough and complete, and will fully convey
the scope of the inventive concept to those skilled in the art. Like numbers refer
to like elements throughout the description.
[0045] Fig. 1 illustrates a medicament delivery device in the first embodiment of the invention
with a housing 1 having a proximal end and a distal end; and a cap assembly 2 arranged
on the proximal end of the housing 1 in an assembled state of the medicament delivery
device. As shown in Fig. 2, the medicament delivery device further comprises: a delivery
member cover 3 axially movable but rotationally fixed in relation to the housing 1;
a resilient member 31 arranged between the distal end of the delivery member cover
3 and an inner distal ledge of housing 1 and configured to bias the delivery member
cover 3 in the proximal direction in relation to the housing 1; a tubular rotator
4, which is a tubular body arranged within the housing 1 and is rotatable but axially
immovable in relation to the housing 1; a plunger rod 5 axially movably arranged within
the housing 1; a drive element 51 arranged within the plunger rod 5 and configured
to bias the plunger rod in the proximal direction; a container carrier 6 arranged
within the housing 1, which is axially and rotationally fixed in relation to the housing
1 and configured to receive a medicament container 8. The medicament container 8 is
configured to contain a medicament and comprises a stopper 81 arranged on its distal
end and a pierceable membrane arranged on its proximal end. A delivery member assembly
7 comprises a delivery member configured to deliver a dose of medicament to the end
user during a medicament delivery operation. The delivery member assembly further
comprises: a delivery member hub configured to hold the delivery member; an inner
cap configured to cover the delivery member; and a retainer configured to threadedly
engage with the inner cap in the assembled state of the medicament delivery device.
The cap assembly 2 is axially fixed to the inner cap of the delivery member assembly
7 and rotationally fixed with the inner cap in unidirectional rotation direction.
[0046] The retainer is snap-fixed to the container carrier 6, such that the cap assembly
2 is attached to the housing 1 through the delivery member assembly 7 in the assembled
state of the medicament delivery device. The cap assembly 2 can be detached from the
housing 1 of the medicament delivery device when the cap assembly 2 and the inner
cap have been both screwed and disengaged from the retainer. Such screwing movement
turns into an axial movement of the delivery member hub due to a coupling between
the inner cap and the delivery member hub whereby the delivery member is moved together
with the delivery member hub towards the medicament container 8 establishing a fluid
communication with the medicament container 8.
[0047] Fig. 3 illustrates the tubular rotator comprising a first retaining member 43a and
a second retaining member 43b arranged on the inner surface of the tubular body. The
first and the second retaining member is configured to selectively engage with the
counter retaining member 52 on the plunger rod 5 as shown in Fig. 4, such that the
proximal axial movement of the plunger rod is prevented. The counter retaining member
52 is configured to rest on the first retaining member 43a when the tubular rotator
4 is in a first rotation position; and is configured to disengage from the first retaining
member 43a and moves proximally under the biasing force of the drive element 51 to
engage with the second retaining member 43b when the tubular rotator 4 is in a second
rotation position.
[0048] The plunger rod 5 is in its initial position when the counter retaining member 52
is engaged with the first retaining member 43a. When the plunger rod is in its initial
position, the medicament delivery device is in its assembled state wherein all components
of the medicament delivery device have been assembled together and the device is ready
to be delivered to an end user. As shown in Fig. 7A, when the medicament delivery
device in the assembled state, there is a gap D defined by the proximal end of the
plunger rod 5 and the distal end of the stopper 81 of the medicament container 8.
Therefore, the risk of accidentally squeezing the stopper 81 forward during shipping
the medicament delivery device and damage the sealing of the medicament container
8 by the plunger rod 5 can be prevented.
[0049] When the counter retaining member 52 of the plunger rod 5 is engaged with the second
retaining member 43b of the tubular rotator 4, the plunger rod 5 is in a calibrated
position, such that the medicament delivery device is also in its calibrated state.
As shown in Fig. 7B, when the medicament delivery device is in its calibrated state,
the proximal end of the plunger rod 5 is configured to be in contact with the stopper
81 of the medicament container 8, such that the gap D between the proximal end of
the plunger rod 5 and the distal end of the stopper 81 is erased.
[0050] When the medicament delivery device is in the calibrated state, a "zero dose" state
is also defined, and the medicament delivery device is now ready to carry out the
medicament delivery operation. The counter retaining member 52 of the plunger rod
5 is then configured to disengage from the second retaining member 43b of the tubular
rotator 4 when the tubular rotator 4 is in a third rotation position, such that the
plunger rod is moved proximally under the biasing force of the drive element 51 and
actuates on the stopper 81 to deliver a dose of medicament. The medicament delivery
operation is therefore started. The counter retaining member 52 of the plunger rod
5 is configured to be proximally moved in order to engage with a dose stop 61 when
the plunger rod 5 is in a final position, such that the medicament delivery operation
is ended. The dose stop 61 can be a ledge arranged on the distal end of the container
carrier 6 as shown in Fig. 5 or a ledge arranged on an extra component or a third
retaining member arranged on the inner surface of the tubular rotator 4. Such that
the delivered dose is determined by the distance between the second retaining member
43b and the dose stop which is also the travel distance of the plunger rod 5 from
the calibrated position to a final position.
[0051] The tubular rotator 4 is configured to interact with the delivery member cover 3.
As shown in Fig. 6A, the delivery member cover 3 comprises a guide element 32 configured
to move along a guide track 41 arranged on the outer surface of the tubular rotator
4. The interaction between the guide element 32 and the guide track 41 forces the
tubular rotator 4 to rotate from the first to the second rotation position; and the
second to the third rotation position.
[0052] As shown in the Fig. 6B, during assembling, the tubular rotator 4 will be assembled
into the housing 1; the delivery member cover 3 and the resilient member 31 will also
be assembled into the housing 1; the guide element 32 will be positioned on a pre-assemble
portion 41a of the guide track 41. Since the delivery member cover 3 is biased by
the resilient member 31, the delivery member cover 3 will protrude from the proximal
end of the housing 1. The last step of assembling is, placing the delivery member
assembly 7 together with the cap assembly 2 towards the proximal end of the housing
1, pressing the proximal end of the delivery member cover 3 against the resilient
member 31 and moving all the delivery member cover 3, the needle assembly 7 and the
cap assembly 2 towards the distal end of the housing until the distal end of the needle
assembly 7 attaches to the container carrier 6, such that the needle assembly 7 is
bidirectional axially fixed with the container carrier 6. Such movement causes the
guide element 32 to move along an assembling path 41b of the guide track 41, until
the distal end of the needle assembly 7 attaches to the container carrier 6 and the
needle assembly 7 together with the delivery member cover 3 no longer can move in
the distal direction in relation to the housing 1. The delivery member cover 3 is
then moved into a first retracted position and compress the resilient member 31 and
the guide element 32 is thereby positioned on a first distal end point 41c. Since
the needle assembly 7 is attached to the container carrier 6, the medicament delivery
device is now properly assembled and is ready for delivering to the end user. When
the medicament delivery device has been assembled, the cap assembly 2 is arranged
on the proximal end of the housing 1, such that the proximal movement of the delivery
member cover 3 is blocked by the cap assembly 2 as shown in Fig. 7A. The guide element
32 is then suspended on the first distal end point 41c of the guide track 41. Once
the cap assembly 2 is detached and completely removed from the housing 1, the delivery
member cover 3 is then moved to its first extended position under the biasing force
of the resilient member 31, such that the proximal end of the delivery member cover
is protruding from the proximal end of the housing 1 and configured to completely
surround the delivery member as shown in Fig. 7B. When the delivery member cover 3
moves into the first extended position, the guide element 32 moves to the proximal
end point 41f of the guide track 41; and passing the first inclined ledge 41d and
the second inclined ledge 41e, such that the tubular rotator 4 is gradually rotated
from the first rotation position to the second rotation position when the guide element
32 passes the first inclined ledge 41d and the second inclined ledge 41e.
[0053] The delivery member cover 3 can be manually pushed distally to its second retracted
position for triggering the medicament delivery operation. When the delivery member
cover 3 moves to the second retracted position, the guide element 32 is moved along
a third inclined ledge 41g and an operation ledge 41h towards its second proximal
distal end point of the guide track 41. When the guide element 32 passes the third
inclined ledge 41g of the guide track 41, the tubular rotator 4 is rotated from the
second rotation position to the third rotation position, such that the medicament
delivery operation is started.
[0054] After the medicament delivery operation is ended, the delivery member cover 3 is
no longer pushed to and retained on the second retraction position; the delivery member
cover 3 is configured to move proximally to its second extended position under the
biasing force of the resilient member 31 and configured to surround the delivery member
again. The proximal movement of the delivery member cover 3 causes the guide element
32 proximally move along the operation ledge 41h of the guide track 41 to its second
proximal end point 41i of the guide track 41. Before the guide element 32 moves into
the second proximal end point 41i of the guide track 41, it passes a locking tongue
42 of the tubular rotator 4, such that the locking tongue 42 comprises a proximally
directed cliff surface, therefore, once the guide element 32 moves into the second
proximal end point 41i of the guide track 41, the further distal movement of the delivery
member cover 3 is prevented due to the blocking between the guide element 32 and the
proximally directed cliff surface of the locking tongue 42.
[0055] The delivery member protrudes from proximal end of the delivery member cover 3 when
the delivery member cover 3 is in the first and the second retracted positions; and
is covered by the delivery member cover 3 when the delivery member cover is in the
first and the second extended positions.
[0056] The axial movement of the delivery member cover 3 driven by the resilient member
31 from the first retracted position to the first extended position causes the guide
element 32 to move from the first distal end point 41c to the proximal end point 41f
of the guide track 41. When the guide element 32 passes the first inclined ledge 41d
and the second inclined ledge 41e, the tubular rotator 4 is gradually rotated from
the first rotation position to the second rotation position.
[0057] It should be noted that, since the rotator 4 is engaged with the plunger rod 5 through
the engagement between the first retaining member 43a and the counter retaining member
52, there will be a friction created between the first retaining member 43a and the
counter retaining member 52 when the rotator 4 is rotating in relation to the plunger
rod 5. The magnitude of the friction is depending on the accumulated force in the
drive element 51, since it applies on the plunger rod 5, if the accumulated force
in the drive element 51 is too high, the rotator 4 might not be rotated by the guide
element 32 of the delivery member cover 3 which is proximally driven by the resilient
member 31. Such a risk can be overcome by arranging a ramp surface to connect the
first and the second retaining member. Therefore, the plunger rod 5 can move along
the ramp surface from the first retaining member 43a to the second retaining member
43b. The rotation of the tubular rotator 4 from the first rotation position to the
second rotation position is thereby mainly under the biasing force from the drive
element 51.
[0058] The medicament delivery device in the first embodiment may further provide an audible/
tactile feedback to the user of the medicament delivery device to indicate the progress
of the medicament delivery operation. The feedback is provided by an interaction member
53 arranged on the plunger rod 5, preferably is a plurality ratchets; and a counter
interaction member 62 arranged on the distal end of the container carrier 6. Once
the plunger rod 5 proximally moves and passes the distal end of the container carrier
6, a continue feedback is thereby generated through the interaction between the interaction
member 53 and the counter interaction member 62.
[0059] Fig. 8A-8B illustrate the second embodiment of the invention. Most of arrangements
in the second embodiment is same as described in the first embodiment. The delivery
member is integral to the proximal end of the medicament container; the cap assembly
2' is arranged to be removed from the housing 1 by an axial pulling movement. The
cap assembly 2' in the second embodiment comprises a gripping element 21' configured
to grip on a groove 33 arranged on the proximal part of the delivery member cover
3. Once the medicament delivery device has been fully assembled, the gripping element
21' of the cap assembly 2 is arranged within the proximal end of the housing 1 and
engages with the groove 33 of the delivery member cover, such that the inner surface
of the proximal end of the housing 1 restricts the gripping element 21' of the cap
assembly 2 from flexing radially outward. The cap assembly 2' is thereby attached
to the housing 1 of the medicament delivery device through the engagement between
the gripping element 21' and the groove 33 arranged on the proximal part of the delivery
member cover 3. The gripping element 21' of the cap assembly 2 is prevented from flexing
radially outward by being blocked by the inner surface of the proximal end of the
housing 1 when the cap assembly 2' is pulled towards the proximal direction in relation
to the housing, for removing the cap assembly 2' from the housing 1, such that the
gripping element 21' will still grip on the groove 33 of the delivery member cover
3 and thereby the delivery member cover 3 is also proximally pulled together with
the gripping element 21' and the cap assembly 2'. Such pulling movement will move
the delivery member cover 3 from the first retracted position to the first extended
position until the gripping element 21' of the cap assembly 2 has been completely
moved out from the housing 1 and the gripping element 21' is able to disengage from
the groove 33 of the delivery member cover 3 by flexing radially outward. The medicament
delivery device is thereby moved from the assembled state to the calibrated state
with the axial cap removal movement. Since the axial movement of the delivery member
cover 3 from the first retracted position to the first extended position and to rotate
the tubular rotator 4 from the first rotation position to the second rotation position,
is mainly under the pulling force by the user of the medicament delivery device, the
resilient member 31 is again no longer needed to accumulate a large force.
[0060] Fig. 9 illustrates a third embodiment of the invention. Most of arrangements in the
third embodiment are the same as described in the first embodiment. The medicament
delivery device in the third embodiment further comprises a rotatable knob assembly
9 arranged on the distal end of the housing 1. As shown in Fig. 10, the knob assembly
9 comprises a user accessible outer knob body 91 and an inner knob body 92. The distal
end of the inner knob body 92 is received within the outer knob body 91 and the proximal
end of the inner knob body 92 is received within the distal portion housing 1. The
inner knob body 92 is axially and rotationally fixed to the outer knob body 91, such
that the inner knob body 92 can be rotated together with the outer knob body 91 by
the end user in relation to the housing 1. The knob assembly 9 is rotatable in relation
to the housing 1 between a first knob position and a second knob position. As shown
in Fig. 12, the inner knob body 92 comprises a holding member 92a configured to hold
the guide element 32, so as the delivery member cover 3 is also hold by the holding
member 92a in the first retracted position when the knob assembly 9 is in the first
knob position. Such that the proximal movement of the delivery member cover 3 is prevented.
[0061] As shown in Fig. 11, the guide track 41' of the tubular rotator 4 in the third embodiment
comprises an initial guide ledge 41a' and a first inclined ledge 41b'. When the user
of the medicament delivery device rotates the knob assembly 9 from the first knob
position to the second knob position, the holding member 92a is misaligned with the
guide element 32, such that the delivery member cover 3 is proximally moved under
the biasing force of the resilient member 31. The guide element 32 therefore moves
along the initial guide ledge 41a' and a first inclined ledge 41b' to the first proximal
end point 41f' of the guide track 41'. Once the guide element 32 passes the first
inclined ledge 41b', the tubular rotator 4 is rotated from the first rotation position
to the second rotation position.
[0062] Fig. 13 illustrates a fourth embodiment of the invention. Most of the arrangements
in the fourth embodiment are the same as described in the third embodiment. The guide
track 41" of the tubular rotator 4 in the fourth embodiment comprises an initial ledge
41a" configured to retaining the guide element 32 of the delivery member cover 3 in
the first retracted position when the medicament delivery device has been properly
assembled and is ready for delivering to the end user. The tubular rotator 4 in the
fourth embodiment further comprises a turning portion 44", configured to engage with
a turning pin 93' arranged on the knob assembly 9 as shown in Fig. 14. When the user
of the medicament delivery device rotates the knob assembly 9, the turning pin 93'
forces the tubular rotator 4 to rotate through the engagement with the turning portion
44". The rotation of the tubular rotator 4 release the guide element 32 from the assembled
ledge 41a", and the delivery member cover 3 is therefore proximally moved to the first
extended position under the biasing force of the resilient member 31. The guide element
32 is moved to its first distal end point 41c" of the guide track 41" and moved along
a curve ledge 41b" of the guide track 41" with the proximal movement of the delivery
member cover 3 towards the first proximal end point 41f" of the guide track 41". Once
the guide element 32 passes the curve ledge 41b", the tubular rotator 4 is rotated
from the first rotation position to the second rotation position.
[0063] Fig. 15A-15B illustrate the medicament delivery device in the assembled state and
the calibrated state in the third and the fourth embodiments of the invention. The
turning movement of the knob assembly 9 from the first knob position, as shown in
Fig. 15A to the second knob position, as shown in Fig. 15B turns the medicament delivery
device from the assembled state to the calibrated state. In the third and the fourth
embodiments the cap assembly 2 is no longer involved the auto calibration mechanism,
so that the cap assembly 2 may be provided with more design flexibility.
[0064] The auto calibration mechanism as described in the first to the fourth embodiment
can also be used with a medicament delivery device with a movable medicament container,
such as the medicament delivery device with auto penetration function. As shown in
Fig. 16, the tubular rotator 4 for a medicament delivery device with auto penetration
function may be modified with a holding arm 45 configured to engage with a holding
shelf 11' arranged on the inner surface of the housing 1 when the medicament delivery
device is in the assembled state and the calibrated state, as shown in Fig. 17. The
tubular rotator may further comprises a connection portion 46 configured to snap on
the distal end counter connection portion of the container carrier 6. So that once
a delivery operation is triggered, the medicament delivery cover 3 turns the rotator
from the second rotation position to the third rotation position with the way described
above, the holding arm 45 will then be moved out from the engagement with the holding
shelf 11'. The tubular rotator 4, the plunger rod 5, the container carrier 6, and
medicament container 8 are thereby moved proximally under the biasing force of the
drive element 51.
[0065] The arrangement of the retaining member of the tubular rotator 4 and the counter
retaining member of the plunger rod 5 can also be arranged in opposite way for the
auto calibration mechanism as described in the first to the fourth embodiment. As
shown in Fig. 18, the counter retaining member of the plunger rod may be modified
as the first counter retaining member 52a' and the second counter retaining member
52b'; the retaining member of the tubular rotator 4 can be modified as a retaining
member 43' as shown in Fig. 19. The first counter retaining member 52a' is configured
to engage with the retaining member 43' on the inner distal surface of the tubular
rotator 4 when the tubular rotator 4 is in first rotation position. When the tubular
rotator 4 moved into the second rotation position, the first counter retaining member
52a' is disengaged from the retaining member 43' and the plunger rod 5 moves proximally
until the second counter retaining member 52b' engaged with the retaining member 43',
such that the medicament delivery device is turned from the assembled state into the
calibrated state.
[0066] The inventive concept has mainly been described above with reference to a few examples.
However, as is readily appreciated by a person skilled in the art, other embodiments
than the ones disclosed above are equally possible within the scope of the inventive
concept, as defined by the appended claims.
[0067] Some other aspects of the invention are defined by the following clauses.
- 1. A medicament delivery device, comprising:
- a housing (1) having a proximal end and a distal end;
- a medicament container (8) arranged within the housing (1) and comprising a stopper
(81) and a delivery member;
- a biased delivery member cover (3) associated with the housing (1) and movable in
relation to the housing (1);
- a biased plunger rod (5) associated with the medicament container (8) and movable
in relation to the housing (1);
- a tubular rotator (4) associated with both the delivery member cover (3) and the biased
plunger rod (5); and
- a cap assembly (2; 2') associated with the housing (1);
wherein a gap (D) is defined between the proximal end of the biased plunger rod (5)
and the stopper (81) of the medicament container (8) when the medicament delivery
device is in an assembled state; and wherein the proximal end of the biased plunger
rod (5) is in contact with the stopper (81) of the medicament container (8) when the
medicament delivery device is in a calibrated state.
- 2. The medicament delivery device according to clause 1, wherein the tubular rotator
(4) comprises a tubular body having at least one retaining member on its inner surface.
- 3. The medicament delivery device according to clause 2, wherein the tubular rotator
(4) comprises a first (43a), a second (43b) and a third retaining member on its inner
surface.
- 4. The medicament delivery device according to clause 2 or 3, wherein the biased plunger
rod (5) comprises a counter retaining element (52) configured to interact with the
at least one retaining member or selectively with each of the first (43a), the second
(43b) and the third retaining members.
- 5. The medicament delivery device according to any one of clause 1 to 4, wherein the
biased delivery member cover (3) comprises a guide element (32); and the tubular rotator
(4) comprises a tubular body arranged with a guide track (41; 41'; 41") on its outer
surface; wherein the guide element (32) is configured to interact with the guide track
(41; 41'; 41") such that an axial movement of the biased delivery member cover (3)
causes the tubular rotator (4) to rotate.
- 6. The medicament delivery device according to clause 5, dependent of clause 4, wherein
the medicament delivery device is in the assembled state when the tubular rotator
(4) is in a first rotation position which is defined when the biased plunger rod (5)
is in an initial position in which the counter retaining element (52) is engaged with
the first retaining member (43a); when the biased delivery member cover (3) is in
a first retracted position in which the guide element (32) is positioned on a first
distal end point (41c) of the guide track (41); and when the biased delivery member
cover (3) is held in said position by the cap assembly (2; 2') which is releasably
connected to the housing (1).
- 7. The medicament delivery device according to clause 5, dependent of clause 4, wherein
the medicament delivery device is in the calibrated state when the tubular rotator
(4) is in a second rotation position which is defined when the biased plunger rod
(5) is in a calibrated position in which the counter retaining element (52) is engaged
with the second retaining member (43b), and when the biased delivery member cover
(3) is in a first extended position in which the guide element (32) is positioned
on a first proximal end point (41f) of the guide track (41) after the cap assembly
(2; 2') is removed from the housing (1).
- 8. The medicament delivery according to clause 6, wherein the biased plunger rod (5)
is configured to move from the calibrated position to a final position in which the
counter retaining element (52) is engaged with the third retaining member, when the
biased delivery member cover (3) is moved from the first extended position to a second
retracted position in which the guide element (32) is positioned on a second distal
end point of the guide track (41) such that the medicament contained in the medicament
container (8) is thereby delivered to a user of the medicament delivery device.
- 9. The medicament delivery device according to clause 7, wherein the biased delivery
member cover (3) is axially movable from the first retracted position to the first
extended position; from the first extended position to the second retracted position;
and from the second retracted position to a second extended position in which the
guide element (32) is positioned on a second proximal end point (41i) of the guide
track (41); such that the delivery member is extended from the delivery member cover
(3) when the delivery member cover is in the first and the second retracted positions;
and is covered by the delivery member cover (3) when the delivery member cover is
in the first and the second extended positions.
- 10. The medicament delivery device according to clause 4, wherein the counter retaining
element (52) is configured to disengage with the second retaining member (43b) when
the biased delivery member cover (3) is axially movable from the first extended position
to the second retracted position such that the tubular rotator (4) is moved from the
second rotation position to a third rotation position.
- 11. The medicament delivery device according to clause 9, wherein the tubular rotator
(4) comprises a ramp surface arranged between the first (43a) and the second (43b)
retaining member; wherein the counter retaining element (52) is configured to move
along the ramp surface from the first retaining member (43a) to the second retaining
member (43b).
- 12. The medicament delivery device according to clause 10, wherein the axial movement
of the biased delivery member cover (3) from the first retracted position to the first
extended position causes the tubular rotator (4) to rotate from the first rotation
position to the second rotation position.
- 13. The medicament delivery device according to any one of preceding clauses, wherein
the medicament delivery device comprises a resilient member (31) configured to proximally
bias the biased delivery cover member (3).
1. A medicament delivery device, comprising:
a plunger rod (5), a drive element (51) arranged within the plunger rod (5) and
configured to bias the plunger rod in a proximal direction;
a container carrier (6) configured to receive a medicament container (8);
wherein an interaction member (53) arranged on the plunger rod (5); wherein a counter
interaction member (62) arranged on a distal end of the container carrier (6) such
that once the plunger rod (5) proximally moves and passes the distal end of the container
carrier (6), a continue feedback is generated through the interaction between the
interaction member (53) and the counter interaction member (62); and wherein the continue
feedback is an audible/tactile feedback configured to indicate the progress of a medicament
delivery operation.
2. The medicament delivery device according to claim 1, wherein the medicament delivery
device comprises a housing (1) having a proximal end and distal end;
wherein the plunger rod (5) is axially movably arranged within the housing (1); and
wherein the container carrier (6) is arranged within the housing (1).
3. The medicament delivery device according to claim 1 or 2, wherein the interaction
member (53) is a plurality ratchets.
4. The medicament delivery device according to any one of the preceding claims, wherein
the medicament delivery device comprises a tubular rotator (4) comprising a first
retaining member (43a) and a second retaining member (43b) arranged on the inner surface
of the tubular body; wherein the first and the second retaining member is configured
to selectively engage with a counter retaining member (52) on the plunger rod (5)
such that the proximal axial movement of the plunger rod is prevented.
5. The medicament delivery device according to claim 4, wherein the counter retaining
member (52) is configured to rest on the first retaining member (43a) when the tubular
rotator (4) is in a first rotation position; and is configured to disengage from the
first retaining member (43a) and moves proximally under the biasing force of the drive
element (51) to engage with the second retaining member (43b) when the tubular rotator
(4) is in a second rotation position.
6. The medicament delivery device according to claim 5, wherein the medicament delivery
device is in an assembled state when the tubular rotator (4) is in the first rotation
position where the counter retaining element (52) is engaged with the first retaining
member (43a); and wherein the medicament delivery device is in a calibrated state
when the tubular rotator (4) is in the second rotation position where the counter
retaining element (52) is engaged with the second retaining member (43b).
7. The medicament delivery device according to claim 6, wherein the plunger rod (5) is
configured to move from the calibrated position to a final position where the counter
retaining element (52) is engaged with a dose stop (61) of the medicament delivery
device.
8. The medicament delivery device according to any one of claims 4-7, wherein the counter
retaining member (52) of the plunger rod (5) is then configured to disengage from
the second retaining member (43b) of the tubular rotator (4) when the tubular rotator
(4) is in a third rotation position such that the medicament delivery operation is
started.
9. The medicament delivery device according to claim 7 or 8, wherein the counter retaining
member (52) of the plunger rod (5) is configured to be proximally moved in order to
engage with a dose stop (61) when the plunger rod (5) is in a final position such
that the medicament delivery operation is ended.
10. The medicament delivery device according to claim 9, wherein the dose stop (61) is
a ledge arranged on the distal end of the container carrier (6).
11. The medicament delivery device according to claim 2 or any one of claims 3-10 when
dependent on claim 2, wherein the tubular rotator is rotatable but axially immovable
in relation to the housing (1).
12. The medicament delivery device according to claim 2 or any one of claims 3-11 when
dependent on claim 2, wherein the medicament delivery device comprises a delivery
member cover (3) movable in relation to the housing (1); wherein the medicament delivery
device comprises a resilient member (31) configured to proximally bias the biased
delivery cover member (3).
13. The medicament delivery device according to claim 12 when dependent on any one of
claims 4-11, wherein the delivery member cover (3) comprises a guide element (32);
and the tubular rotator (4) comprises a tubular body arranged with a guide track (41)
on its outer surface; wherein the guide element (32) is configured to interact with
the guide track (41) such that an axial movement of the biased delivery member cover
(3) causes the tubular rotator (4) to rotate.
14. The medicament delivery device according to claim 13 when dependent on claims 6-11,
wherein the counter retaining element (52) is configured to disengage with the second
retaining member (43b) when the delivery member cover (3) is axially movable from
a first extended position to a second retracted position such that the tubular rotator
(4) is moved from the second rotation position to the third rotation position.
15. The medicament delivery device according to claim 14, wherein the delivery member
cover (3) is held in a first retracted position where the guide element (32) is positioned
on a first distal end point (41c) of the guide track (41) by a cap assembly (2) of
the medicament delivery device; and wherein the delivery member cover (3) is in the
first extended position where the guide element (32) is positioned on a first proximal
end point (41f) of the guide track (41) after the cap assembly (2) is removed from
the housing (1).